Search results for "Microscopy"

showing 10 items of 3390 documents

Hedysarum coronarium-Based Green Composites Prepared by Compression Molding and Fused Deposition Modeling

2022

In this work, an innovative green composite was produced by adding Hedysarum coronarium (HC) flour to a starch-based biodegradable polymer (Mater-Bi®, MB). The flour was obtained by grinding together stems, leaves and flowers and subsequently sieving it, selecting a fraction from 75 μm to 300 μm. Four formulations have been produced by compression molding (CM) and fused deposition modeling (FDM) by adding 5%, 10%, 15% and 20% of HC to MB. The influence of filler content on the processability was tested, and rheological, morphological and mechanical properties of composites were also assessed. Through CM, it was possible to obtain easily homogeneous samples with all filler amounts.…

biocompositesTechnologyMicroscopyQC120-168.85FDMgreen compositesTQH201-278.5biopolymers3D printingnatural fillerEngineering (General). Civil engineering (General)ArticleMater-BiTK1-9971Settore ING-IND/22 - Scienza E Tecnologia Dei MaterialiDescriptive and experimental mechanicsgreen composites; biocomposites; FDM; biopolymers; Mater-Bi; natural filler; additive manufacturing; 3D printingGeneral Materials ScienceElectrical engineering. Electronics. Nuclear engineeringTA1-2040additive manufacturing3D printing Additive manufacturing Biocomposites Biopolymers FDM Green composites Natural filler Mater-BiMaterials; Volume 15; Issue 2; Pages: 465
researchProduct

Creep Behavior of Poly(lactic acid) Based Biocomposites

2017

Polymer composites containing natural fibers are receiving growing attention as possible alternatives for composites containing synthetic fibers. The use of biodegradable matrices obtained from renewable sources in replacement for synthetic ones is also increasing. However, only limited information is available about the creep behavior of the obtained composites. In this work, the tensile creep behavior of PLA based composites, containing flax and jute twill weave woven fabrics, produced through compression molding, was investigated. Tensile creep tests were performed at different temperatures (i.e., 40 and 60 °C). The results showed that the creep behavior of the composites is strongly inf…

biocomposites; PLA; flax; jute; creepMaterials scienceflaxjuteCompression molding02 engineering and technologyBiocomposites; Creep; Flax; Jute; PLA010402 general chemistry01 natural scienceslcsh:TechnologyArticlecreepchemistry.chemical_compoundUltimate tensile strengthGeneral Materials ScienceComposite materiallcsh:Microscopylcsh:QC120-168.85biocompositeslcsh:QH201-278.5lcsh:TAdhesion021001 nanoscience & nanotechnology0104 chemical sciencesLactic acidSynthetic fiberSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiCreepchemistrylcsh:TA1-2040Polymer compositesPLAlcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineering0210 nano-technologylcsh:Engineering (General). Civil engineering (General)Biocompositelcsh:TK1-9971Materials
researchProduct

Effects of tributyltin(IV) chloride on fertilization ofStyela plicata(Ascidiacea: Tunicata): II. Scanning and transmission electron microscopy studies

2003

The morphological aspects of Styela plicata fertilization after treatment with tributyltin(IV) chloride are described by means of scanning and transmission electron microscopy investigations. Alterations have been shown both on female and male gametes; spermatozoa, all the egg envelopes and the mitochondria of the egg cortical cytoplasm are modified in relation to incubation time. As a consequence, the damage to gametes blocks sperm–egg interaction and fertilization does not occur. Copyright © 2003 John Wiley & Sons, Ltd.

biologyChemistryMineralogyGeneral Chemistrybiology.organism_classificationChlorideCell biologyInorganic Chemistrychemistry.chemical_compoundStyela plicataHuman fertilizationCytoplasmTransmission electron microscopymedicineTributyltinFertilisationAscidiaceamedicine.drugApplied Organometallic Chemistry
researchProduct

Surface Modification of Porous Polyethylene Implants with an Albumin-Based Nanocarrier-Release System

2021

Background: Porous polyethylene (PPE) implants are used for the reconstruction of tissue defects but have a risk of rejection in case of insufficient ingrowth into the host tissue. Various growth factors can promote implant ingrowth, yet a long-term gradient is a prerequisite for the mediation of these effects. As modification of the implant surface with nanocarriers may facilitate a long-term gradient by sustained factor release, implants modified with crosslinked albumin nanocarriers were evaluated in vivo. Methods: Nanocarriers from murine serum albumin (MSA) were prepared by an inverse miniemulsion technique encapsulating either a low- or high-molar mass fluorescent cargo. PPE implants …

biologyChemistryQH301-705.5release kineticsSerum albuminbiomaterialMedicine (miscellaneous)Biomaterialfluorescence microscopyGeneral Biochemistry Genetics and Molecular BiologyArticlematerial scienceMiniemulsionTissue engineeringIn vivoporous polyethylenetissue engineeringbiology.proteinSurface modificationImplantNanocarriersBiology (General)dorsal skinfold chamberalbumin nanocarriersBiomedical engineeringBiomedicines
researchProduct

Transmission Electron Microscopy of GroEL, GroES, and the Symmetrical GroEL/ES Complex

1994

Two new 2-D crystal forms of the Escherichia coli chaperone GroEL (cpn60) 2 x 7-mer have been produced using the negative staining-carbon film (NS-CF) technique. These 2-D crystals, which contain the cylindrical GroEL in side-on and end-on orientations, both possess p21 symmetry, with two molecules in the respective unit cells. The crystallographically averaged images correlate well with those obtained by other authors from single particle analysis of GroEL and our own previous crystallographic analysis. 2-D crystallization of the smaller chaperone GroES (cpn10) 7-mer has also been achieved using the NS-CF technique. Crystallographically averaged images of GroES single particle images indic…

biologyChemistrySingle particle analysisChaperonin 60GroESChromatography Ion ExchangeGroELlaw.inventionModels StructuralMicroscopy ElectronCrystallographyMolecular geometryStructural BiologylawChaperone (protein)Chaperonin 10Escherichia colibiology.proteinMoleculeProtein quaternary structureCrystallizationCrystallizationJournal of Structural Biology
researchProduct

Structure of keyhole limpet hemocyanin type 1 (KLH1) at 15 Å resolution by electron cryomicroscopy and angular reconstitution † 1 †This article is de…

1997

Abstract A three-dimensional reconstruction of keyhole limpet hemocyanin type 1 (KLH1) has been obtained using electron cryomicroscopy at liquid helium temperatures and single particle image processing. The use of a high-contrast embedding medium, 1% (w/v) glucose and 2% (w/v) ammonium molybdate (pH 7.0), enables high-resolution electron micrographs to be recorded close to focus, i.e. with excellent transfer of high-resolution information, while maintaining enough image contrast to localise the individual macromolecules in the images. When low-pass filtered to ∼45 A resolution, the new 15 A resolution reconstruction is very similar to the earlier reconstructions of gastropodan hemocyanins o…

biologyCryo-electron microscopymedicine.medical_treatmentResolution (electron density)Single particle analysisHemocyaninMegathura crenulatabiology.organism_classificationSymmetry (physics)CrystallographyStructural Biologybiology.proteinmedicineMolecular BiologyKeyhole limpet hemocyaninMacromoleculeJournal of Molecular Biology
researchProduct

Labeling of Single Cells in the Central Nervous System of <em>Drosophila melanogaster</em>

2013

In this article we describe how to individually label neurons in the embryonic CNS of Drosophila melanogaster by juxtacellular injection of the lipophilic fluorescent membrane marker DiI. This method allows the visualization of neuronal cell morphology in great detail. It is possible to label any cell in the CNS: cell bodies of target neurons are visualized under DIC optics or by expression of a fluorescent genetic marker such as GFP. After labeling, the DiI can be transformed into a permanent brown stain by photoconversion to allow visualization of cell morphology with transmitted light and DIC optics. Alternatively, the DiI-labeled cells can be observed directly with confocal microscopy, …

biologyGeneral Immunology and MicrobiologyGeneral Chemical EngineeringGeneral NeuroscienceCellbiology.organism_classificationCell morphologyEmbryonic stem cellMolecular biologyeye diseasesGeneral Biochemistry Genetics and Molecular BiologyCell biologyGreen fluorescent proteinlaw.inventionmedicine.anatomical_structureSingle-cell analysisConfocal microscopylawmedicinesense organsDrosophila melanogasterDevelopmental biologyJournal of Visualized Experiments
researchProduct

Immunological and ultrastructural characterization of spirotrichonymphid flagellates from Reticulitermes grassei and R. flavipes (syn. R. santonensis…

2006

AbstractFive species of spirotrichonymphids representing three genera have been studied by light and immunofluorescence microscopy, and by transmission electron microscopy. The genus Spirotrichonympha, represented by S. flagellata from Reticulitermes grassei, is characterized by a compound axostyle composed of several fibers or subaxostyles. The genus Spironympha, represented by S. kofoidi from Reticulitermes flavipes (syn. R. santonensis) and by the two new species S. verticis and S. lanceata, is characterized by flagellar lines restricted to the anterior area and a simple, tubular axostyle. Spironympha verticis and S. lanceata are mainly distinguished by ultrastructural details of their f…

biologyImmunofluorescenceImmunofluorescence MicroscopyBiodiversitybiology.organism_classificationTermitesReticulitermesGenusSpirotrichonymphaUltrastructureBotanyParabasaliaReticulitermes grasseiUltrastructureProtozoaAxostyleProtozoaEcology Evolution Behavior and Systematics
researchProduct

Electron microscopy and biochemical characterization of a 350-kDa annular hemolymph protein from the keyhole limpet Megathura crenulata

1994

The isolation and biochemical characterization of an annular non-hemocyanin hemolymph protein from a marine gastropod, the Californian giant keyhole limpet (Megathura crenulata) is presented. By analytical ultracentrifugation, the protein has a sedimentation coefficient of 12S and molecular mass of approximately 350 kDa. The subunit mass, obtained by SDS/PAGE in the presence of -SH reagent and 8 M urea, is approximately 35 kDa, thereby indicating the presence of 10 subunits in the native molecule. By negative staining, the protein is revealed in one predominant image projection as a pentagonal approximately 8 nm ring-like structure with an approximately 2-nm stain-filled centre and, in anot…

biologyMolecular massProtein Conformationmedicine.medical_treatmentProtein subunitLimpetProteinsHemocyaninMegathura crenulatabiology.organism_classificationBiochemistryNegative stainMolecular WeightMicroscopy ElectronCrystallographyMolluscaHemolymphLimulusHemolymphmedicineBiophysicsAnimalsElectrophoresis Polyacrylamide GelUltracentrifugationEuropean Journal of Biochemistry
researchProduct

Protection of living yeast cells by micro-organized shells of natural polyelectrolytes

2015

International audience; Saccharomyces cerevisiae, a eukaryotic model organism, plays a key role in the oxidative stability of fermented products. In order to protect cells against environmental stresses, we report a method of modifying the cell surface architecture while maintaining the internal working properties of the system. The objective was to encapsulate living yeast cells in micro-organized polyelectrolyte shells using layer-by-layer (LbL) assembly. For the first time, the natural polyelectrolytes, β-lactoglobulin and sodium alginate, were alternately deposited on the surface of S. cerevisiae. Transmission electron microscopy coupled with immune-cytochemistry and scanning electron m…

biologyScanning electron microscopeChemistrySaccharomyces cerevisiaeLayer by layerBioengineeringSaccharomyces cerevisiaebiology.organism_classificationLayer-by-layerβ-LactoglobulinApplied Microbiology and BiotechnologyBiochemistryPolyelectrolyteYeastBiochemistryFTIRTransmission electron microscopyFreezing[SDV.IDA]Life Sciences [q-bio]/Food engineeringBiophysicsFermentation[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringFourier transform infrared spectroscopyImmuno-electron microscopy
researchProduct